TY - JOUR
T1 - Amikacin inhalation as salvage therapy for refractory nontuberculous mycobacterial lung disease
AU - Jhun, Byung Woo
AU - Yang, Bumhee
AU - Moon, Seong Mi
AU - Lee, Hyun
AU - Park, Hye Yun
AU - Jeon, Kyeongman
AU - Jung Kwon, O.
AU - Ahn, Jungmin
AU - Moon, Il Joon
AU - Shin, Sung Jae
AU - Daley, Charles L.
AU - Koh, Won Jung
N1 - Publisher Copyright:
Copyright © 2018 American Society for Microbiology. All Rights Reserved.
PY - 2018/7
Y1 - 2018/7
N2 - Although guidelines recommend amikacin (AMK) inhalation therapy for difficult-to-treat nontuberculous mycobacterial lung disease (NTM-LD), data are limited regarding the safety and clinical efficacy of this salvage therapy. We retrospectively evaluated the treatment outcomes of 77 patients with refractory NTM-LD caused by Mycobacterium abscessus complex (MABC) or M. avium complex (MAC) who initiated AMK inhalation therapy between February 2015 and June 2016. MABC was the most common etiology (n 48, 62%), followed by MAC (n 20, 26%) and mixed infections (n 9, 12%). Isolates with macrolide resistance and baseline AMK resistance were identified in 63 (82%) patients and 5 (6%) patients, respectively. At 12 months after AMK inhalation therapy, 49% of patients had symptomatic improvement, whereas 42% had radiological improvement. Conversion to a negative sputum culture occurred in 14 (18%) patients, and the culture conversion rate was higher in patients infected with macrolide-susceptible isolates (7/14, 50%) than in those infected with macrolide-resistant isolates (7/63, 11%) (P 0.003). Significant decreases in sputum semiquantitative culture positivity occurred after AMK inhalation therapy (P 0.001). On multivariate analysis, conversion to a negative sputum culture was associated with mixed infections (P 0.009), a forced expiratory volume in 1 s of greater than 60% (P 0.008), and the absence of macrolide resistance (P 0.003). Thirty-eight percent of patients experienced adverse effects, with ototoxicity (n 15) being the most common. AMK inhalation salvage therapy may improve the treatment responses in some patients with refractory NTM-LD. However, considering the common adverse effects, further evaluation of the optimal dosage and intervals for AMK inhalation therapy is needed.
AB - Although guidelines recommend amikacin (AMK) inhalation therapy for difficult-to-treat nontuberculous mycobacterial lung disease (NTM-LD), data are limited regarding the safety and clinical efficacy of this salvage therapy. We retrospectively evaluated the treatment outcomes of 77 patients with refractory NTM-LD caused by Mycobacterium abscessus complex (MABC) or M. avium complex (MAC) who initiated AMK inhalation therapy between February 2015 and June 2016. MABC was the most common etiology (n 48, 62%), followed by MAC (n 20, 26%) and mixed infections (n 9, 12%). Isolates with macrolide resistance and baseline AMK resistance were identified in 63 (82%) patients and 5 (6%) patients, respectively. At 12 months after AMK inhalation therapy, 49% of patients had symptomatic improvement, whereas 42% had radiological improvement. Conversion to a negative sputum culture occurred in 14 (18%) patients, and the culture conversion rate was higher in patients infected with macrolide-susceptible isolates (7/14, 50%) than in those infected with macrolide-resistant isolates (7/63, 11%) (P 0.003). Significant decreases in sputum semiquantitative culture positivity occurred after AMK inhalation therapy (P 0.001). On multivariate analysis, conversion to a negative sputum culture was associated with mixed infections (P 0.009), a forced expiratory volume in 1 s of greater than 60% (P 0.008), and the absence of macrolide resistance (P 0.003). Thirty-eight percent of patients experienced adverse effects, with ototoxicity (n 15) being the most common. AMK inhalation salvage therapy may improve the treatment responses in some patients with refractory NTM-LD. However, considering the common adverse effects, further evaluation of the optimal dosage and intervals for AMK inhalation therapy is needed.
UR - http://www.scopus.com/inward/record.url?scp=85049048887&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85049048887&partnerID=8YFLogxK
U2 - 10.1128/AAC.00011-18
DO - 10.1128/AAC.00011-18
M3 - Article
C2 - 29661870
AN - SCOPUS:85049048887
SN - 0066-4804
VL - 62
JO - Antimicrobial agents and chemotherapy
JF - Antimicrobial agents and chemotherapy
IS - 7
M1 - e00011-18
ER -